Products

Wemedoo’s oomnia system integrates powerful tools including CTMS, EDC, eTMF, ePRO, eCOA, eConsent, eSource, and RTSM, enabling end-to-end oversight and seamless collaboration across the clinical trial lifecycle.

Patient pre-screening AI assistant for clinical trial recruitment.

All-in-one Physician AI tool. Contains trained medical chatbot, Ambient Physician Copilot, AI Clinical Documentation and Medical code extractor. Newly introduced: DICOM Medical Imaging Viewer and AI Analysis

Sarjen offers three specialized solutions for clinical trial management and lab automation. The Early Phase CTMS (BizNET) and Late Phase CTMS (Smart Trial Suite) are clinical trial management systems that streamline and automate early and late-phase trials, respectively. They ensure compliance, enhance data integrity, and reduce operational costs through features like intelligent automation and seamless integration. The Bioanalytical LIMS is a lab information management system that automates wor

Clinical trial management system

Health Studio is a clinical data platform built exclusively on Google Cloud. This low code platform allows organizations to build AI-enabled clinical solutions in a fraction of the time, unlocking all Google cloud resources and APIs with clicks not code. This allows organizations to introduce AI-enabled workflows and agent based applications with lower risk and cost and accelerate the time to realize the benefits. Further Health Studio's modular and customizable design integrates with existing t

Tapt Health completes your documentation while you treat. Leverage AI to better engage patients, expedite evals, and minimize after-hours documentation.

Lyfeguard is the client management software solution for modern financial advisers. We empower advisers with client-centric, cutting-edge technology designed to deepen connections with clients.

RealTime-Devana is a holistic business intelligence platform designed specifically for research site organizations, driving transparency and accountability across all functional groups. From pipeline management and streamlined study start-up through to historical trial metrics, Devana provides one source of truth for all your clinical trial data and processes. Improve turnaround times and stand out to CROs and sponsors with Devana’s powerful workflow improvements and data analytics.

Delve Health combines eCOA/ePRO, wearable device integration, real-time analytics, and Concierge-as-a-Service™ into one clinical trial execution platform. Designed for sponsors, CROs, and research sites running hybrid and decentralized studies, Delve achieves 92–98% ePRO completion rates through proactive patient outreach in 120+ languages, device compliance monitoring, signal quality control, and site burden reduction. Used across oncology, CNS, cardiovascular, rare disease, respiratory, and po

An application for managing expanded access and compassionate use programs — covering request intake, medical review, ethics approval, regulatory filing, and logistics coordination.

inTrial Manage is the operating system for plaintiff trial firms. We replace the fragmented stack most firms duct-tape together — case management, client intake, eSign, e-fax, texting, team chat, and document storage — with one purpose-built platform. AI handles the work that used to eat your team's day: medical chronologies built in seconds, demand letters drafted from your case file, complaints generated on command. Built by plaintiff lawyers who were tired of paying for software that was neve

Chronicles eCRF is a configurable SaaS solution which may be set up by clients in strict compliance with the protocol in both interventional (Phase I-IV and BE/BA) studies and non-interventional programs. • Integrated randomization, stratification and blinding. • Built-in trial supply management tools. • Study-specific form builder with edit checks, lab ranges, and multi-language support. • MedDRA and ATC coding, CDISC/CDASH-ready datasets. • Compatibility with modern statistical softwar

Catchtrial® EDC+ is a next-generation clinical trial platform combining data capture, imaging, safety workflows, and AI-driven analytics in one integrated, secure environment. It enables real-time oversight, faster decision-making, and the delivery of high-quality, approval-ready data across global studies. Catchtrial® EDC+ serves as an intelligent clinical trial governance environment, where investigators, core labs, safety adjudication teams, monitors, and statisticians collaborate around r

Medigen® CTMS+ centralizes planning, monitoring, document management, product oversight and finances to streamline trials, reduce costs, and deliver faster, smarter results.

CDISC-based fast eCRF production with AI technology. Provides customized EDCs. GAMP5 certification as an integrated platform for clinical trial data management. 21 CFR Part 11, Annex 11 Certification ISO900:2015 Certification 24/7 Global Service Support Team Quick trial start and affordability compared to other systems

Nabla leverages machine learning to revolutionize patient relationships and streamline clinical documentation.

Medigen Suite offers a premier collection of intuitive clinical research solutions designed to streamline complex clinical trials. Their products include Electronic Data Capture, Clinical Trial Management Systems, and ePRO/eCOA applications, catering to various trial phases and sizes. The company targets organizations involved in clinical research, providing accessible and reliable cloud-based tools to enhance trial efficiency. With a focus on transforming the research experience, Medigen Suite